多路复用
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
病毒
生物
冠状病毒
病毒学
2019年冠状病毒病(COVID-19)
传输(电信)
计算生物学
生物信息学
医学
计算机科学
疾病
传染病(医学专业)
电信
病理
作者
Courtney Vedelago,Junrong Li,Kym Lowry,Christopher B. Howard,Alain Wuethrich,Matt Trau
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2023-04-07
卷期号:8 (4): 1648-1657
被引量:13
标识
DOI:10.1021/acssensors.2c02782
摘要
Severe acute respiratory syndrome coronavirus 2 variants play an important role in predicting patient outcome during postinfection, and with growing fears of COVID-19 reservoirs in domestic and wild animals, it is necessary to adapt detection systems for variant detection. However, variant-specific detection remains challenging. Surface-enhanced Raman scattering is a sensitive and multiplexing technique that allows the simultaneous detection of multiple targets for accurate identification. Here we propose the development of a multiplex SERS microassay to detect both the spike and nucleocapsid structural proteins of SARS-CoV-2. The designed SERS microassay integrates gold–silver hollow nanobox barcodes and electrohydrodynamically induced nanomixing which in combination enables highly specific and sensitive detection of SARS-CoV-2 and the S-protein epitopes to delineate between ancestral prevariant strains with the newer variants of concern, Delta and Omicron. The microassay allows detection from as low as 20 virus/μL and 50 pg/mL RBD protein and can clearly identify the virus among infected versus healthy nasopharyngeal swabs, with the potential to identify between variants. The detection of both S- and N-proteins of SARS-CoV-2 and the differentiation of variants on the SERS microassay can aid the early detection of COVID-19 to reduce transmission rates and lead into adequate treatments for those severely affected by the virus.
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